Document 6478345
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Document 6478345
Blackwell Publishing IncMalden, USAJSMJournal of Sexual Medicine1743-6095© 2006 International Society for Sexual Medicine200635923931Original ArticleSurgical Treatment of Vulvar VestibulitisGoldstein et al. 923 ORIGINAL RESEARCH—SURGERY Surgical Treatment of Vulvar Vestibulitis Syndrome: Outcome Assessment Derived from a Postoperative Questionnaire Andrew T. Goldstein, MD,*† Daisy Klingman, MD,‡ Kurt Christopher, MD,§ Crista Johnson, MD,¶ and Stanley C. Marinoff, MD, MPH** *Division of Gynecologic Specialties, Department of Gynecology and Obstetrics, Johns Hopkins Medicine, Baltimore, MD; † Center for Vulvovaginal Disorders, Washington, DC; ‡Department of Psychiatry, University of Pittsburgh Medical Center, Pittsburgh, PA; §Department of Obstetrics and Gynecology, St. Luke’s-Roosevelt Medical Center, New York, NY; ¶ Department of Obstetrics and Gynecology, University of Michigan Medical School, Ann Arbor, MI; **Department of Obstetrics and Gynecology, George Washington University School of Medicine, Washington, DC, USA DOI: 10.1111/j.1743-6109.2006.00303.x ABSTRACT Introduction. Vulvar vestibulitis syndrome (VVS) is the most common pathology in women with sexual pain. Surgery for VVS was first described in 1981. Despite apparently high surgical success rates, most review articles suggest that surgery should be used only “as a last resort.” Risks of complications such as bleeding, scarring, and recurrence of symptoms are often used to justify these cautionary statements. However, there are little data in the peer-reviewed literature to justify this cautionary statement. Aims. To determine patient satisfaction with vulvar vestibulectomy for VVS and the rate of complications with this procedure. Methods. Women who underwent a complete vulvar vestibulectomy with vaginal advancement by one of three different surgeons were contacted via telephone by an independent researcher between 12 and 72 months after surgery. Main Outcome Measures. The primary outcome measurement of surgical success was overall patient satisfaction with surgery. Additional secondary outcome measurements included improvement in dyspareunia, changes in coital frequency, and occurrence of surgical complications. Results. In total, 134 women underwent surgery in a 5-year period. An independent research assistant was able to contact 106 women, and 104 agreed to participate in the study. Mean duration since surgery was 26 months. A total of 97 women (93%) were satisfied, or very satisfied, with the outcome of their surgery. Only three patients (3%) reported persistently worse symptoms after surgery and only seven (7%) reported permanent recurrence of any symptoms after surgery. Prior to surgery, 72% of the women were completely apareunic; however, after surgery, only 11% were unable to have intercourse. Discussion. In this cohort of patients, there was a high degree of satisfaction with surgery for VVS. In addition, the risks of complications with this procedure were low, and most complications were transient and the risk of recurrence after surgery was also found to be low. Goldstein AT, Klingman D, Christopher K, Johnson C, and Marinoff SC. Surgical treatment of vulvar vestibulitis syndrome: Outcome assessment derived from a postoperative questionnaire. J Sex Med 2006;3:923–931. Key Words. Vaginal Reconstructive Surgery; Causes and Treatment of Sexual Pain Disorders; Dyspareunia © 2006 International Society for Sexual Medicine J Sex Med 2006;3:923–931 924 Figure 1 Vestibular erythema in vulvar vestibulitis syndrome. Introduction V ulvar vestibulitis syndrome (VVS) (vestibulodynia, vestibular adenitis, localized vulvar dysesthesia) is one of the most common causes of sexual pain in women [1,2]. Patients with VVS experience severe introital dyspareunia that is frequently described as burning, cutting, or searing, upon vaginal penetration. Pain is localized to the tissue of the vulvar vestibule which is derived from the primitive urogenital sinus (Figure 1) [3]. Women who have had introital dyspareunia ever since their first attempt at intercourse (or tampon insertion) have primary VVS, whereas women who had an initial interval of pain free intercourse prior to the onset of symptoms are described as having secondary VVS. While the underlying pathophysiology of VVS has not been completely elucidated, several recent studies have confirmed a proliferation of c-afferent nociceptors in the vestibular mucosa [4–8]. These studies have shown up to a 10-fold increase in density of nerve endings in the vestibular mucosa of women with VVS [5]. This neuronal hyperplasia may explain the extreme allodynia women experience with VVS. Recent studies have suggested that in some cases, primary VVS may be the result of a congenital neuronal hyperplasia in the tissue derived from the primitive urogenital sinus [9,10]. Additional studies have suggested that secondary VVS may be caused by nerve growth factor-initiated proliferation of nociceptors mediated by mast cells [5]. J Sex Med 2006;3:923–931 Goldstein et al. Additional factors such as genetic polymorphisms in genes, down-regulation of hormonal receptors, or hormonal alterations caused by oral contraceptive pills may also play a role in the pathogenesis of VVS [11–14]. There are more than 20 different treatments reported in the medical literature for VVS, including topical and intra-lesional steroids [15], interferon [16], biofeedback [17], capsaicin [18], lidocaine [19], intravaginal physical therapy [20], amitriptyline [21], cognitive–behavioral therapy [22], acupuncture [23], nitroglycerine [24], and dietary changes [25]. Safety and efficacy data concerning these treatment regimens are published, for the most part, in small case series, which are neither randomized nor placebo-controlled. Woodruff first described surgery for VVS in 1981 calling it a “modified perineoplasty” [26]. Since that time, there have been 32 different case series compromising a total of 1,275 patients (Table 1). These reports represent several different surgical procedures as there have been modifications of the basic excision and reconstructive procedure. In the original procedure, Woodruff removed a semicircular segment of perineal skin, the mucosa of the posterior vulvar vestibule, and the posterior hymeneal ring. Three centimeters of the vaginal mucosa was then undermined and approximated to the perineum. While there are flaws in the peer-reviewed publications that examine surgery for VVS, 28 of the 32 articles demonstrate at least an 80% success Table 1 Sexual functioning after vulvar vestibulectomy surgery N (%) Quality of sex life (N = 104) Much better/better Same Worse Current level of pain during sex (N = 104) No pain Discomfort that does not interference with sex Discomfort that does with interference sex Apareunia Sexual activity 3 months prior to surgery (N = 104) None 1–2 times/month 2–3 times/month Sexual activity since surgery (N = 104) None 1–2 times/month 2–3 times/month Ability to achieve orgasm (N = 104) Increased Decreased No change 91 (87) 11 (11) 2 (2) 54 26 12 12 (52) (25) (12) (12) 77 (74) 20 (19) 7 (7) 12 (11) 34 (33) 58 (56) 10 (10) 9 (9) 85 (81) Surgical Treatment of Vulvar Vestibulitis 925 rate with surgical management of VVS [27]. Yet, despite this apparently high success rate, most review articles and lectures suggest that surgery should be used only “as a last resort” [28–30]. Risks of complications such as bleeding, infection, wound dehiscence, hematoma, scarring, increased pain, unfavorable cosmesis, inhibition of orgasm, Bartholin’s gland cyst formation, and recurrence of symptoms are often used to justify these cautionary statement. However, there is very little available peer-reviewed medical literature to quantify rates of complications with surgery for VVS. This information is essential to accurately counsel women contemplating surgery for VVS. Materials and Methods In total, 134 women had vulvar vestibulectomy with vaginal advancement performed by one of three different gynecologic surgeons between October 1, 1997 and October 1, 2003. Women were considered candidates for surgery if they had pain limited to the vulvar vestibule. They were excluded if they had vulvar pain that was not limited to the vestibule (dysesthetic vulvodynia [DV]), or they had pelvic floor muscle hypertonicity (PFMH) (pelvic floor dysfunction, vaginismus). Although the women were not required to have used conservative treatments prior to surgery, 99 of the 104 women tried at least one conservative treatment prior to surgery. A woman was considered a candidate for surgery if she, and her surgeon, determined that she was willing and capable to follow the postoperative care outlined below. In addition, she had to have at least two thorough discussions about available conservative treatment options prior to consenting to surgery. A psychological consultation was not a prerequisite for surgery. The procedure performed on all women was a modification of the original Woodruff procedure. Modifications of the original procedure were developed by the three surgeons to minimize complications that have been associated with the original procedure [31]. Specifically, the entire vulvar vestibule is outlined and then infiltrated with Marcaine 0.5% with epinephrine for intraoperative hemastasis and postoperative pain control (Figure 2). The mucosa of the anterior vestibule is excised even when this area is not painful as this lowers the chance of postoperative symptom recurrence. The mucosa of the entire vestibule is then excised to a point 3 millimeters past the hymenal ring, thereby removing the entire hymen. Figure 2 The entire vulvar vestibule is outlined prior to excision. The vaginal mucosa is then separated off the recto-vaginal fascia to create a vaginal advancement flap (Figure 3). The defects in the anterior vestibule are then closed with 4–0 Vicryl and the vaginal mucosa is then anchored in an advanced position with six mattress stitches of 2–0 Vicryl. These mattress stitches are positioned in an anterior-posterior direction so that the diameter of the Figure 3 After excising the vestibular mucosa, a vaginal advancement flap is created. J Sex Med 2006;3:923–931 926 Goldstein et al. dential, and that their surgeon would be blinded to individual responses. A thorough chart review was performed after contacting individual patients. Results Figure 4 The vaginal advancement flap is approximated to the perineum. vagina is not compromised. The mattress stitches minimize the risk of postoperative hematoma, prevent curling of the advancement flap, and minimize the risk of dehiscence of the advancement flap. The procedure is completed by approximating the vaginal mucosa to the labia minora and perineum with approximately 20 interrupted stitches of 4–0 Vicryl (Figure 4). Using interrupted stitches minimizes the risks of hematoma, wound dehiscence, and postoperative scarring. All patients applied ice to the perineum postoperatively for 7 days, used Sitz baths for 6 weeks, and remained on modified bed-rest for 2 weeks. Six weeks after surgery, the women began vaginal dilatation with Pyrex dilators. Patients were contacted between 12 and 72 months after their surgery (mean 26 months). Patients were contacted by an independent research assistant via telephone. The research assistant, a medical student on a research elective, attempted to contact the patients with telephone numbers that were in the medical record. If the telephone numbers were no longer valid, an Internet search engine was used to find current phone numbers. Of the 134 women who had undergone surgery in the aforementioned 6-year period, 106 of the women were contacted (79%). An IRBapproved questionnaire was administered by the independent research assistant after obtaining verbal informed consent (Appendix 1). Participants were assured that their responses would be confiJ Sex Med 2006;3:923–931 Ninety-one women (87%) reported that their sex lives were much better or better than before surgery. Eleven women (11%) reported no change in their sex and two (2%) women reported that their sex lives were worse since surgery (Table 1). In the 3 months prior to surgery, 77 women (74%) were apareunic because of severe dyspareunia, and 20 of the remaining 27 women (19%) had intercourse no more than twice monthly. After the surgery, 58 women (56%) were having intercourse at least three times per month, and only 12 women (11%) were apareunic. Eighty-five women (81%) did not have any change in their ability to achieve orgasm after surgery, 10 women (10%) had an increased ability to achieve orgasm and nine women (9%) had decreased ability to achieve orgasm. Eighty-seven women (83%) reported no recurrence of symptoms of dyspareunia after surgery, whereas 10 women (10%) had transient recurrence of dyspareunia, and seven (7%) had permanent recurrence of dyspareunia (Table 2). Ninetyfour women (90%) reported no worsening of symptoms from the surgery; whereas seven women (7%) had transient worsening of symptoms and three (3%) had some permanent worsTable 2 Patient satisfaction with surgical outcomes N (%) Recurrence of symptoms (N = 104) Yes—transient Yes—permanent No 10 (10) 7 (7) 87 (83) Symptoms made worse by surgery (N = 104) Yes—transiently Yes—permanently No 7 (7) 3 (3) 94 (90) Cosmetic changes (N = 104) Very significant Significant Not significant 3 (3) 4 (4) 97 (93) In retrospect, knowing your results and discomfort of surgery, would you have surgery again (N = 104) Yes No Unsure 97 (93) 3 (3) 4 (4) Would you recommend surgery to another woman with similar symptoms (N = 104) Yes No Unsure 97 (93) 1 (1) 6 (6) 927 Surgical Treatment of Vulvar Vestibulitis ening of symptoms. Ninety-seven women (93%) considered the cosmetic results of the surgery to be insignificant, whereas four women (4%) considered them significant and three women (3%) considered the cosmetic results to be very significant. Ninety-seven patients (93%) answered that in retrospect, knowing the discomfort of their surgery, and the results of their surgery, they would have the surgery again, and would also recommend the surgery to other women with similar complaints. No patients had postoperative infection, significant wound dehiscence, or significant scarring. Table 3 Procedure Woodruff et al. [26] Woodruff and Parmley [40] Woodruff and Friedrich [41] Peckham [42] Friedrich [43] Michlewitz [44] Bornstein and Kaufman [45] Perineoplasty Perineoplasty Perineoplasty Perineoplasty Perineoplasty Perineoplasty Perineoplasty (modified) Perineoplasty Modified vestibulectomy Vestibuloplasty Perineoplasty Modified vestibulectomy Vestibulectomy Perineoplasty Perineoplasty Perineoplasty (modified) Perineoplasty Vestibulectomy Vestibuloplasty Modified vestibulectomy Vestibulectomy Vestibulectomy Vestibulectomy Perineoplasty Vestibulectomy Perineoplasty Modified vestibulectomy Vestibulectomy Perineoplasty Perineoplasty Vestibulectomy Vestibulectomy Modified vestibulectomy Vestibulectomy Marinoff and Turner [46] Westrom [47] Schover [48] Mann [49] Barbaro [50] Abramov [51] Bornstein [52] Foster [53] Chaim [54] de Jong [55] Baggish [56] Goetsch [57] Kehoe [58] Weijmar [59] Bergeron [60] Bergeron [22] Bornstein [34] Berville [61] Marinoff [62] Westrom [6] Kehoe [63] Hopkins [64] McKormack [65] Schneider [66] Gaunt [67] Lavy [68] Total Discussion A review of the 32 studies that have examined surgery for VVS reveals that the surgical success rate was greater than 80% in 28 of these studies (Table 3). However, these studies are frequently criticized because the outcome criteria for “surgical success” are often poorly defined and standard procedures to assess surgical success are rarely Review of vestibulectomy studies Authors Traas [69] One patient had a hematoma that required evacuation, and two patients had a Bartholin’s gland cyst that required in-office marsupialization. Partial (significant) resolution of pain No significant resolution of pain Complete or significant reduction in pain 0 2 6 0 0 0 2 0 15 4 2 100 100 95 100 60 100 90 60 10 11 1 2 1 97 92 1–24 6–54 1–3 18 37 19 14 12 2 6 7 84 88 100 7 11 93 16 12 6 >48 10–70 7 9 51 15 1 31 1 11 1 14 15 12 37 36–84 12 6–72 3–34 3 13 10 22 3 8 2 13 38 22 79 12 107 42 2–36 13–120 6 12 8 3–48 6 7 24 15 60 6 70 33 54 21 42 54 42 59 2–42 NS 12–120 6 6–24 6–120 33 19 16 30 28 39 126 2–264 76 Length of follow-up (in months) Complete resolution of pain 18 14 44 9 38† 16 20 6–60 6–36 NS* NS NS NS 6–36 18 12 36 9 23 16 14 73 12 12–36 15–19 38 56 21 Number of patients 2 11 4 4 43 87 100 89 2 19 4 85 68 68 100 83 82 90 19 15 10 7 6 2 7 9 4 7 89 90 83 83 90 87 37 13 89 19 4 18 5 15 2 14 7 100 91 88 94 1,275 *NS: length of follow-up not stated. † Includes 13 patients who had a previous failed surgery performed by another surgeon. J Sex Med 2006;3:923–931 928 used. In addition, evaluation of success in these studies is non-blinded, rendering it biased and highly subjective. Therefore, this study was designed to address the aforementioned deficiencies. In this study, several specific outcome measurements were used to assess surgical success. The primary measure of success was overall patient satisfaction with surgery. Additional secondary outcome measurements included resolution or significant improvement in dyspareunia, increased coital frequency, and absence of surgical complications. In this cohort of patients, 93% of patients were satisfied, or very satisfied, with their surgical outcome. The authors believe that this very high level of satisfaction was achieved for several reasons. As with any surgical procedure, patient selection is extremely important. It has been shown in the literature that women with active DV and/or PFMH have a lower surgical success rate [32–34]. Therefore, women with DV or PFMH were not offered surgery until these concurrent problems were successfully treated. Forty-three of the 106 women had one or both of these conditions upon initial presentation, but were successfully treated for DV or PFMH prior to undergoing surgery. In addition, modifications of the original Woodruff procedure described above minimize the risks of postoperative hematoma, wound dehiscence, and postoperative scarring. Modified bed-rest for the 2 weeks after the procedure minimizes postoperative complications and aggressive use of vaginal dilators beginning 6 weeks after surgery prevents postoperative vaginal stenosis and leads to early resumption of intercourse. This study is one of the first to quantify the risks that are frequently mentioned when discussing this procedure. These data will allow physicians to accurately discuss the risks of this procedure when deciding on treatment options with their patients or when obtaining informed consent for this procedure. This study was limited because it did not incorporate validated measures of assessing sexual function such as use of the Female Sexual Function Index and Female Sexual Distress Scale at various time intervals pre- as well as postoperatively. In addition, in future studies age-matched controls with VVS who choose not to undergo surgery should be compared with women who have surgery along dimensions of sexual functioning and quality of life measures. Furthermore, women who made the decision to undergo surgery may have experienced cognitive J Sex Med 2006;3:923–931 Goldstein et al. dissonance reduction and biased scanning in response to questions on the questionnaire which elicited whether they would undergo surgery again knowing the discomforts and surgical outcomes. The concepts of cognitive dissonance reduction and biased scanning assume that the influence of one’s past behavior on future decisions is mediated by attempts to confirm the legitimacy of the behavior once one becomes aware of its occurrence, and this can occur with very little thought about the behavior in question and the consequences of engaging in it [35]. Janis and King [36] first postulated the theory of biased scanning wherein after people have engaged in a particular behavior, they often conduct a biased search of memory for previously acquired knowledge that confirms the legitimacy of their act. They may then combine their estimates of the likelihood and desirability of these consequences to form a new attitude toward the behavior [37], and this attitude, in turn, might influence both their intentions to repeat the behavior and their actual decision to do so when the occasion arises [35]. The theory of cognitive dissonance assumes that when people become aware that they have voluntarily performed a behavior that contradicts the implications of a previously formed attitude, they experience discomfort (dissonance) [38,39]. Therefore, they attempt to rationalize their counter-attitudinal behavior by convincing themselves that they had good reasons for engaging in it. This rationalization is likely to produce a change in their estimates of both the likelihood and desirability of the behavior’s specific consequences and therefore a revision of the attitude for which these estimates have implications. The new attitude, in turn, may provide the basis for their future behavioral decisions [35]. In this study, biased scanning and cognitive dissonance reduction may have been introduced in women who underwent vulvar vestibulectomy with vaginal advancement. Based on these theories, patients with VVS may still recommend a surgical intervention for other women in order to create less dissonance, even if their surgical outcome may in fact have been either unfavorable or resulted in no change in their current health status. Lastly, while there have been several recent studies showing promising new treatment for VVS including topical lidocaine [18] and capsaicin [17], it is not known whether these treatment options temporize the symptoms of VVS or offer a longterm cure for VVS. As the majority of women with Surgical Treatment of Vulvar Vestibulitis VVS are in the third decade of life, it is important to question the benefit of treatment options that are palliative rather than curative. Therefore, until there is evidence that there are other treatments for VVS that offer cure rates that are comparable to surgery, vestibulectomy should not be reserved as a treatment of last resort. 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Eur J Obstet Gynecol Reprod Biol 2005;120:91–5. 69 Traas MA, Bekkers RL, Dony JM, Blom M, van Haren AW, Hendriks JC, Vierhout ME. Surgical treatment for the vulvar vestibulitis syndrome. Obstet Gynecol 2006;107(2 Pt 1):256–62. Appendix 1 Telephone Interview Questionnaire 1. In retrospect, knowing the discomforts of surgery and the results of your surgery, would you have surgery again? Yes/No/Unsure. 2. Knowing the discomforts of surgery and the results of your surgery, would you recommend this surgery to another woman with similar symptoms? Yes/No/Unsure. 3. In general, is your sex life—much better, better, the same, or worse, as compared with before the surgery? Much better/Better/Same/Worse. 4. What is your current level of pain during sex: 0—no pain, 1—discomfort that does not interfere with sex, 2—discomfort that frequency interferes with sex, 3—unable to have sex? Or N/A—not in a relationship. 5. Were any symptoms made worse by the surgery? Yes/No. If yes, what were they? 6. In the last 3 months, on average, how many times did you have intercourse per month? 7. Have you had a recurrence of your symptoms since having surgery? If yes, what were they and do these symptoms persist? 8. Has your ability to have orgasm been affected by this surgery? Increased/Decreased/Same. 9. Would you consider the cosmetic changes associated with the procedure to be: very significant, significant, not significant? J Sex Med 2006;3:923–931